Fixation device for surgical repair

ABSTRACT

A method and apparatus for performing a surgical repair may involve fixation of a repair material, such as a ligament or tendon in knee ligament repair procedure, to an internal cortical contact area in a bone. The cortical bone contact area may be located immediately adjacent an opening in the bone&#39;s surface through which the repair material extends. The repair material may be engaged with the contact area by way of a fixation device, such as a device that is attached to the repair material and functions as a stop member. An illustrative fixation device may include an annular portion with an aperture through with the repair material passes. The repair material may be attached to a securing portion that extends from the annular portion.

BACKGROUND OF INVENTION

1. Field of Invention

This invention relates to methods and apparatus for surgical repair.

2. Discussion of Related Art

Fixation devices are often used for surgical repair, such as whenattempting to secure one body portion relative to another or relative toa surgical implant or other device. For example, tendon or ligamentdamage frequently requires surgery for repair, e.g., to reattach a tornor separated tendon or ligament to the bone to which the tendon/ligamentwould normally be attached. Knee ligament injuries typically involvedamage to one or more ligaments such that a ligament, or at least aportion thereof, requires reattachment to the tibia and/or femur. FIG. 1shows a schematic diagram of a knee 1 and a portion of a ligament 2(e.g., an anterior cruciate ligament, or ACL, that is normally attachedbetween the femur 1 1 and the tibia 12. In one type of damage to theligament 2, the ligament 2 may detach or be partially torn from thefemur 11 and/or tibia 12, such as that shown schematically in FIG. 2.Such damage may be repaired by replacing the ligament 2 with a graft orother repair material, as is known in the art. One repair technique forreplacing the ligament 2 involves drilling holes 13 in both the femur 11and tibia 12, and fixing the graft 14 in both holes, e.g., usinginterference screws 14 as shown in FIG. 3.

SUMMARY OF INVENTION

In one aspect of the invention, a ligament repair technique is providedthat does not necessarily require the use of an interference screw tosecure the ligament to a bone. In one embodiment, a portion of the boneitself may support the ligament without the need for an interferencescrew or other fixation device. In another embodiment, a fixationdevice, if provided, may be positioned in contact with an interior bonesurface, e.g., a cortical bone surface, to secure the ligament in place

In one aspect of the invention, a surgical repair method includesforming an opening in a first bone, with the opening having a first sizeat an outer surface of the first bone. For example, the first bone maybe a tibia, and the opening may be formed in a portion of the tibia nearwhere a knee ligament, such as an ACL, is normally attached. A contactarea is then formed inside the first bone, with the contact area beingformed, at least in part, by cortical bone located near the openinginside the first bone's outer surface and having a size that is largerthan the first size. For example, the contact area may be formed by anannular surface of the cortical bone inside the tibia and surroundingthe opening. A first end of a joint repair material may be secured tothe contact area in the opening, and the joint repair material may bepositioned to extend from within the first bone at the contact area outthrough the opening. For example, a graft ligament may be secured to thecontact area and extend out of the opening toward the femur. A secondend of the joint repair material opposite the first end may be securedto a body member distinct from the first bone, e.g., the graft ligamentmay be secured to a femur, thereby connecting the tibia and femur.Although in this example the joint repair material is a graft ligament,the joint repair material may be any suitable naturally-occurringmaterial (such as an autograft or allograft material), a syntheticmaterial, or any suitable combination of natural and syntheticmaterials.

In another aspect of the invention, a surgical repair method includesforming a passageway through a bone with respect to which a joint repairmaterial is to be fixated such that the passageway extends from a firstopening to a second opening. A contact area may be formed inside thebone, so that the contact area is defined, at least in part, by corticalbone located inside the bone's outer surface near the second opening. Afirst side of the joint repair material may be secured to a fixationdevice, and the fixation device may be positioned within the bone sothat the fixation device is seated at the contact area and the jointrepair material extends out of the second opening. In one illustrativeembodiment, the passageway may be formed through a tibia so that thesecond opening and contact area are located near the knee joint. Thejoint repair material, e.g., a graft ligament, may be secured to afixation device and fed into the passageway such that the fixationdevice engages the contact area (securing the graft relative to thetibia) and the graft extends from the second opening. The graft may besecured to a femur using any suitable technique to complete the ligamentrepair. Thus, the fixation device may engage the contact area so thatthe fixation device resists tension placed on the joint repair materialto pull the joint repair material from the passageway and out of thesecond opening.

The passageway may be formed so that the second opening has a smallersize than the first opening. In one embodiment, the passageway may beformed by forming a hole through the bone, with the hole having a sizeapproximately equal to the size of the second opening. A counterbore maybe formed in the hole to form the first opening and the contact area.Cancellous bone in the passageway may be displaced (e.g., compacted,removed, etc.) to expose an area of cortical bone in the passageway.

In another aspect of the invention, a surgical fixation device includesa base portion with an aperture constructed and arranged to receive ajoint repair material, such as a graft ligament. The base portion has acontact surface and is constructed and arranged to contact a bone at thecontact surface and secure the joint repair material relative to thebone. The fixation device also may include a securing portionconstructed and arranged to secure the joint repair material relative tothe base portion. The securing portion is arranged to engage with thebase portion on a side of the base portion opposite the contact surface.The base portion and the securing portion may be arranged to be deployedentirely within a bone opening, e.g., such that no portion of thefixation device is located outside of the bone, and to resist tensionapplied on the joint repair material secured to the securing portion ina direction from the securing portion toward the contact surface. Inaddition, the securing portion may be arranged to position the jointrepair material in contact with bone in the bone opening, e.g., toencourage attachment of the graft to the bone by healing processes.

In another aspect of the invention, a surgical fixation device includesan annular portion having a bone contact surface on a first side and anopening adapted to receive a ligament repair material. A securingportion may be arranged to engage with a second side of the annularportion opposite the first side. The securing portion may have anelongated member extending in a direction away from the contact surfacewhen engaged with the annular portion, and may be adapted to secure aligament repair material passing through the opening to the annularportion. The annular portion and the securing portion may be arranged tobe deployed entirely within a bone opening and to resist tension appliedon the ligament repair material secured to the securing portion in adirection from the securing portion toward the contact surface.

In one embodiment, at least a portion of the securing portion extendsacross the opening in the annular portion. Also, the elongated member ofthe securing portion may include opposed grooves to receive the jointrepair material, and may have one or more openings adapted to receivesuture to secure the ligament repair material to the securing portion.The elongated member of the securing portion may have a Y-shape with twolegs attached to the annular portion (e.g., on opposite sides of theopening) and one leg extending away from the annular portion. Thesecuring portion may also taper so as to be thinner in a region near theopening in the flange and so as to be thicker in a region positionedaway from the opening. The base and securing portions may be made of anon-absorbable, biocompatible material, such as titanium, and/or anabsorbable material, such as polylactic acid (PLA), and/or othermaterials or combinations of materials.

Other aspects of the invention are provided that are not necessarilyrestricted to use in knee ligament repair. Instead, aspects of theinvention may be used in other surgical repair techniques in which aligament, tendon, prosthetic or other material is secured relative tobone.

BRIEF DESCRIPTION OF DRAWINGS

Various aspects of the invention are described with reference toillustrative embodiments, wherein like numerals reference like elements,and wherein:

FIG. 1 is a schematic diagram of a knee and attached ligament;

FIG. 2 is a schematic diagram of a knee with a ligament injury;

FIG. 3 is a schematic diagram of a ligament repair arrangement inaccordance with known repair techniques;

FIG. 4 shows a schematic diagram of a ligament repair in accordance withaspects of the invention;

FIG. 5 shows a schematic diagram of a ligament repair in which therepair material includes an integrally formed fixation member;

FIG. 6 shows a schematic diagram of an opening formed in a bone in oneillustrative embodiment;

FIG. 7 shows a schematic diagram of a repair material being inserted into an opening formed like that in FIG. 6;

FIG. 8 shows a perspective view of a fixation device in an illustrativeembodiment;

FIG. 9 shows a bottom view of the fixation device of FIG. 8;

FIG. 10 shows a top view of the fixation device of FIG. 8;

FIG. 11 shows a side view of the fixation device of FIG. 8 with a repairmaterial attached;

FIG. 12 shows a perspective view of a fixation device in anotherillustrative embodiment;

FIG. 13 shows a front view of a fixation device in yet an illustrativeembodiment;

FIG. 14 shows a side view of the fixation device of FIG. 13;

FIG. 15 shows a top view of the fixation device of FIG. 13; and

FIG. 16 shows a cross sectional view of the fixation device along theline 16-16 in FIG. 13.

DETAILED DESCRIPTION

This invention is not limited in its application to the details ofconstruction and the arrangement of components set forth in thefollowing description or illustrated in the drawings. The invention iscapable of other embodiments and of being practiced or of being carriedout in various ways. Also, the phraseology and terminology used hereinis for the purpose of description and should not be regarded aslimiting.

Various aspects of the invention are described below with reference tospecific embodiments. For example, aspects of the invention aredescribed in the context of performing a knee ligament repair. However,it should be understood that aspects of the invention are notnecessarily restricted to knee ligament repair techniques, or even tosurgical techniques performed on a knee. Rather, various aspects of theinvention may be used in any suitable surgical procedure. In addition,various aspects of the invention may be used alone, and/or incombination with any other aspects of the invention.

FIG. 4 shows a schematic diagram of a surgical repair in accordance withaspects of the invention. As discussed above, although aspects of theinvention are described with reference to a knee ligament repair forease of reference and understanding, aspects of the invention may beused in any surgical or other procedure, and may involve any suitablebody portions, such as bone, muscle, other tissue or combinationsthereof, vascular structures, digestive structures, medical implants orother devices, etc. Thus, aspects of the invention are in no way limitedto the specific embodiments and examples described herein.

In this illustrative embodiment, a ligament 2, such as an anteriorcruciate ligament (ACL) 2 has been damaged and is replaced by a repairmaterial 4. The repair material 4 may be an allograft or autograft ofknee ligament material, such as ligament material harvested from apatient's patella or a harvested hamstring tendon, etc. The repairmaterial 4 may optionally be a man-made material, such as a mesh orother prosthetic device. In short, the repair material 4 may be anysuitable material or combination of materials for the repair.

In accordance with one aspect of the invention, one end of the repairmaterial 4 is secured relative to a bone via contact with an internalarea of cortical bone. Thus, the repair material 4 may be robustly fixedin place without necessarily requiring an interference screw, anexpanding anchor, or other similar device. In this illustrativeembodiment, the repair material 4 engages with an internal contact area5 of the tibia 12, but it should be understood that a similar engagementmay be made with a contact area 5 in the femur 11. By engaging therepair material 4 with a cortical bone contact area 5, the repairmaterial 4 can be solidly anchored relative to the bone with a minimalrisk of movement of the contact area 5, e.g., in the direction oftension tending to pull the repair material 4 out of the tibia 12 andtoward the femur 11. This is not necessarily the case with anchoringarrangements that engage the repair material 4 with cancellous bone,which may compress or otherwise give way when the repair material 4 isplaced under tension or other stress.

The contact area 5 may be formed in the bone in any suitable way. Forexample, in the embodiment shown in FIG. 4, a passageway 6 may beinitially formed through the tibia 12 such that the passageway 6 has anapproximately constant diameter from a first opening 61 to a secondopening 62 near the knee joint. This passageway 6 may be formed in anysuitable way, such as those known in the art including drilling,punching or other. Thereafter, the passageway 6 may be counterbored in adirection from the first opening 61 toward the second opening 62 so thatthe first opening 61 has a larger diameter than the second opening 62.The counterbore may be formed by using a drill of a larger size than thepassageway's initial size, a reaming tool, a punch, etc. The contactarea 5 may be formed by the tool used to form the counterbore, or may beformed separately, such as by a tamping device, reamer, etc. thatcrushes and/or moves cancellous bone so as to expose a cortical bonearea to serve as the contact area 5. The contact area 5 may have anannular shape and be arranged in a plane that is perpendicular (orotherwise generally transverse) to the longitudinal axis of thepassageway 6 (or to the general direction in which tension is applied tothe repair material 4). However, the contact area 5 is not limited toflat, annular arrangements, but instead may have a conical orsemi-conical shape, may be rectangular, oval, triangular, etc. Also, thecontact area 5 need not necessarily be flat, but may have bumps, ridges,grooves or other features.

The repair material 4 may be secured to the contact area 5 in anysuitable way, such as by one or more fixation devices that are formedseparately from and attached to the repair material, and/or by acomponent that is integrally formed with the repair material. Forexample, the repair material 4 may be secured to a bushing-like memberor other device that has at least one portion that is larger than thesize of the second opening 62. As a result, if the repair material 4 isfed through the passageway 6 from the first opening 61 and pulledthrough the second opening 62, the bushing-like member may engage withthe contact area 5, preventing the repair material 4 from being furtherpulled from the second opening 62.

In another illustrative embodiment, the repair material may have anintegrally formed member that engages with the contact area 5. Forexample, as shown in FIG. 5, an autograft ligament 4 that is harvestedfrom a patient's patella tendon may include bone blocks on either end ofthe tendon. The bone blocks may be shaped or otherwise suitably arrangedso that a bone block at a first end 41 of the tendon may pass throughthe second opening 62, allowing the tendon portion to be pulled throughthe second opening 62 as well. However, the bone block at the second end42 of the tendon may be larger than the second opening 62, and thusengage with the contact area 5 to secure the tendon in place. In anotherembodiment, a synthetic repair material may include an integrally formedstop member or other portion that engages with the contact area 5.

In another illustrative embodiment, the opening formed in the bone forsecuring a repair material need not be formed as a passageway thatextends from one opening through the bone to another opening. Instead,as shown in FIG. 6, the opening 6 may partially extend into the bone 12,and be arranged so that a contact area 5 is provided beneath the outersurface of the bone 12. In this embodiment, the opening 6 may be formedin any suitable way, such as by first drilling a hole into the bone, andthen enlarging the size of the hole beneath the surface of the bone toform the contact area 5 in the bone's cortical region. The repairmaterial 4 may be secured in the opening 6 in any suitable way, such asby an expanding anchor-type fixation device that is secured to therepair material 4, inserted through the opening, and then expands atleast in part to engage the contact area 5. In another embodiment, theopening 6 may be formed to have an oblong or other suitable shape asshown in FIG. 7. The repair material 4 may have a complementary fixationdevice 7 that is inserted through the opening 6, and then rotated in theopening 6 so that the fixation device 7 engages the contact area 5 andprevents the fixation device 7 from being pulled from the opening 6. Thefixation device 7 may be formed in any suitable way. For example, thefixation device 7 may be a suitably shaped bone block that is part of aharvested patella tendon, as described above. Alternately, the fixationdevice 7 may be a separately formed component that is secured to aligament or other repair material 4.

FIG. 8 shows a schematic view of a fixation device 7 in one illustrativeembodiment. The fixation device 7 includes a base portion 71, which inthis embodiment is an annular-shaped flange, with a contact surface 72arranged to engage with the contact area 5 in a bone. The base portion71 includes an aperture 73 to receive a ligament or other repairmaterial 4. Although in this embodiment, the base portion 71 is shown toform a closed loop around the aperture 73, the base portion 71 need notdo so, and may have one or more splits or gaps in the base portion 71.Also, the base portion 71 need not have an annular shape as shown, butmay have an oval, rectangular, triangular, elongated or other suitableshape. Generally, the contact surface 72 will be flat, but may bearranged in other ways, such as to include serrations, bumps, grooves orother suitable features.

A securing portion 74 may have an elongated shape and extend from thebase portion 71 in a direction away from the contact surface 72. One ormore holes 75 or other features may be provided in the securing portion74, e.g., to receive suture for securing a repair material 4 to thesecuring portion 74. As can be seen in the bottom view of FIG. 9, thesecuring portion 74 may include opposed grooves 76 to receive the repairmaterial 4. Also, the securing portion 74 may taper along a centralregion from the distal end (farthest from the base portion 71 as shownin FIG. 9) to a proximal end (nearest the base portion 71 as shown inthe top view of FIG. 10). This taper may help in passing the repairmaterial through the aperture 73 (because of the relatively smallthickness of the securing portion 74 near the aperture 73) and inpositioning the repair material 4 against the walls of the bone opening(the thicker portion of the securing portion 74 may urge the repairmaterial 4 into contact with the bone at and near the distal end) toencourage ingrowth of the bone or otherwise encourage healing processesthat secure the repair material 4 to the bone. Thus, in one embodiment,the securing portion 74 may have a Y-shape with two legs attached to thebase portion 71 and another leg extending away from the base portion 71.

FIG. 11 shows a repair material 4 (in this example a ligament graft)engaged with the fixation device 7 of FIGS. 8-10. The repair material 4passes through the aperture 73 and extends along a first groove 76 ofthe securing portion 74. The repair material 4 then extends over thedistal end of the securing portion 74 and down the opposed second groove76 and through the aperture 73. (In another embodiment, two strands ofrepair material 4 may pass through the aperture 73 and extend alongopposed grooves 76 of the securing portion 74, terminating distally ofthe distal end of the securing portion 74.) Suture, clips or othersecuring material (not shown) may engage the repair material 4 and thesecuring portion 74 at the holes 75 or otherwise to help keep the repairmaterial 4 in place relative to the fixation device 7. In oneillustrative embodiment, the repair material 4 may have a diameter ofabout 8-11 mm, with the aperture 73 having approximately the same size(e.g., 8-11 mm) and the outer diameter of the base portion 71 beingabout 10-15 mm. The length of the securing portion 74 may be about 10-25mm, or more or less, as suitable for the application. The fixationdevice 7 may be made of any material or suitable combination ofmaterials, including non-absorbable/biocompatible materials (such astitanium, stainless steel, other alloys, etc.), absorbable materials(such as PLA, PGA, reprocessed bone, and other materials, mixtures orcomposites), or combinations of materials. The fixation device 7 mayalso be coated with or otherwise include materials that encourage bonegrowth, such as an osteo-conductive or osteo-inductive material.

Although in this embodiment, the fixation device 7 is shown as formed asa unitary piece, e.g., molded of a suitable material, the fixationdevice 7 may be made in two or more separate parts. For example, thebase portion 71 and the securing portion 74 may be made separately andassembled on a repair material. The securing portion 74 may then engagethe base portion 71 by way of interference to resist pulling of therepair material 4 and the securing portion 74 through the aperture 73.For example, in an application like that shown in FIG. 7, the repairmaterial may first threaded through the aperture 73 of a base portion71, and then engaged with a separate securing portion 74. Thereafter,the securing portion 74 and repair material 4 may be inserted into theopening 6, followed by the base portion 71 being inserted in the opening6. The base portion 71 may be arranged in the form of a split ring(e.g., a flat annular washer-like device with a cut or gap) such thatthe base portion 71 may be forced through the opening 6 (e.g., byfolding or deforming the base portion 71 to reduce its size). The baseportion 71 may then be oriented to engage the contact area 5 and thesecuring portion 74 may be seated against the base portion 71 to securethe repair material 4. In another embodiment, the base portion 71 mayhave an oval, rectangular, oblong or other shape such that the baseportion 71 may be passed through the opening 6, and then turned orotherwise oriented so that the base portion 71 cannot be pulled throughthe opening 6.

In other illustrative embodiments, the securing portion 74 may includetwo or more portions to help secure the repair material 4, to helpengage the repair material with bone in the opening, and/or to performother functions. For example, the securing portion 74 may include asleeve that is located over the repair material 4 after the material 4is engaged with the securing portion 74 as shown in FIG. 11. The sleevemay help secure the repair material 4 in place, as well as helpencourage bone ingrowth. In another embodiment, the securing portion 74may be made to expand in diameter, e.g., when tension is placed on therepair material after deployment of the fixation device 7. Expansion ofthe securing portion 74 may help urge the repair material 4 into contactwith the bone in the walls of the opening 6. Expansion may occur as aresult of the design of the securing portion 74, e.g., the securingportion may be made hollow or otherwise deformable in at least a portionso that the securing portion 74 buckles outwardly with tension appliedto the repair material. Alternately, insertion of an interference pin,screw or other device into the securing portion 74 may expand a portionof the securing portion 74 and force the repair material into contactwith the wall of the opening. In other embodiments, the repair material4 may be secured to the securing portion 74 using interference screws orpins, or other devices.

In the embodiments above, the repair material 4 is first secured at thecontact area 5, e.g., of the tibia 12, and then an opposite, second endof the repair material 4 is secured to another bone, e.g., the femur 11.However, it should be understood that aspects of the invention are notso limited. Instead, the repair material 4 may be first secured (e.g.,to a tibia 12) using the techniques described above or any othersuitable method, and then secured to a cortical contact area 5 (e.g., ina femur 11). Although securing of the repair material to the contactarea 5 may be performed using the devices described above, FIG. 12 showsanother illustrative embodiment of a fixation device 7 that allows fortensioning of the repair material, and subsequent fixation to the device7. The fixation device 7 may be constructed largely as described abovewith a base portion 71 and securing portion 74. With the base portion 71seated against the contact area 5, the repair material 4 may be pulledthrough the aperture 73 (with the fixation device 7 held in contact withthe contact area 5 of the bone) until suitable tension is applied.Thereafter, a sleeve 78 may be engaged over the securing portion 74 andthe repair material 4 to secure the repair material 4 to the securingportion 74. This securing operation may be performed in other ways aswell. For example, the securing portion 74 may be formed as a sleeve orcylindrical member with the repair material 4 passing through theinterior of the sleeve. To secure the repair material 4 in place, aninterference pin, screw or other member may be inserted into the sleeve,forcing the repair material into contact with the securing portion 74.The securing portion 74 may have slots or other openings to allow tissueingrowth.

FIGS. 13-16 show front, side, top and sectional views of a fixationdevice 7 in another illustrative embodiment. This embodiment is similarto that shown in FIGS. 8-11, but has a cylindrically shaped part thatincludes an annular base portion 71 with an annular contact surface 72.The securing portion 74 has a wedge-like shape and extends approximatelydiametrically across the aperture 73 defined by the base portion 71.Although in this embodiment the securing portion 74 does not includegrooves 76 or holes 75 like that in the FIGS. 8-11 embodiment, suchfeatures may be included if desired. This embodiment has the followingdimensions, although it should be appreciated that the dimensions may bevaried as desired: an overall height H1 of about 15 mm, a base height H2of about 4 mm, an intermediate height H3 of about 10 mm, an upper heightH4 of about 5 mm, an upper groove depth H5 of about 2 mm, a securingportion upper thickness T of about 2 mm, an overall diameter D1 of about11 mm, and an inner diameter D2 of about 10 mm. Although not shown, inthis embodiment the base portion 71 may include a separate washer orother device (e.g., shaped like the base portion 71 shown in FIG. 8 andthat is separate from the cylindrical part) that contacts the baseportion 71 at the contact surface 72 and engages the contact area 5 ofthe bone. The washer may be split (e.g., like a conventional lock washerused with bolts or screws) to allow the washer to be reduced in size andinserted into an opening 6. Thereafter, the washer may expand to itsoriginal shape to engage with the contact area 5 and provide anengagement surface for the base portion 71.

It should be understood that aspects of the invention include repairtechniques in which a repair material is secured to a cortical contactarea 5 of a bone at one or more ends of the repair material. Moreover,if one portion of a repair material 4 is secured to a cortical contactarea 5, other portions of the repair material 4 may be secured to thesame or different bone using any suitable technique or device, as areknown in the art, such as interference screws, etc. In addition,fixating a repair material via a cortical contact area may besupplemented by additional securing techniques, such as conventionalinterference screw fixation.

Although various embodiments have been described above in the context ofa knee ligament repair, aspects of the invention may be used in otherapplications, such as rotator cuff repair or other tendon repair, herniamesh fixation, and others.

Having thus described several aspects of at least one embodiment of thisinvention, it is to be appreciated various alterations, modifications,and improvements will readily occur to those skilled in the art. Suchalterations, modifications, and improvements are intended to be part ofthis disclosure, and are intended to be within the spirit and scope ofthe invention. Accordingly, the foregoing description and drawings areby way of example only.

1. A surgical fixation device, comprising: a base portion including anaperture constructed and arranged to receive a joint repair material,the base portion having a contact surface and being constructed andarranged to contact a bone at the contact surface and secure the jointrepair material relative to the bone surface; and a securing portionconstructed and arranged to secure the joint repair material to the baseportion, the securing portion being arranged to engage with the baseportion on a side of the base portion opposite the contact surface andextending away from the base portion, the securing portion having a partthat extends across the aperture; wherein the base portion and thesecuring portion are arranged to be deployed entirely within a boneopening and to resist tension applied on the joint repair materialsecured to the securing portion in a direction from the securing portiontoward the contact surface, the securing portion being arranged toposition the joint repair material in contact with bone in the boneopening.
 2. The device of claim 1, wherein the part of the securingportion that extends across the aperture tapers so as to be thinner in aregion near the aperture and so as to be thicker in a region positionedaway from the aperture.
 3. The device of claim 1, wherein the securingportion has an elongated shape that extends away from the base portion.4. The device of claim 1, wherein the base portion includes a circularflange with an annular contact surface.
 5. The device of claim 1,wherein the base portion includes a circular aperture.
 6. The device ofclaim 1, wherein the securing portion includes opposed grooves toreceive the joint repair material.
 7. The device of claim 1, wherein thesecuring portion includes one or more openings adapted to receive sutureto secure the joint repair material to the securing portion.
 8. Thedevice of claim 1, wherein the base portion includes a cylindricalportion that defines the aperture, and where the securing portion has awedge-like shape that is fixed to the cylindrical portion and extendsacross the aperture.
 9. The device of claim 1, wherein the aperture isdefined by a closed loop of the base portion, and the securing portionextends across the aperture.
 10. The device of claim 9, wherein thesecuring portion tapers so as to be thinner in a region near theaperture and so as to be thicker in a region positioned away from theaperture.
 11. The device of claim 1, wherein the base and securingportions are made of an i absorbable material.
 12. The device of claim1, wherein the base and securing portion are adapted to be used in aknee ligament repair procedure.
 13. The device of claim 1, wherein thebase and securing portion are adapted to be used in a knee ligamentrepair procedure using subcortical bone fixation of the ligament. 14.The device of claim 1, wherein the base portion includes a washerelement having an annular shape, that defines the contact surface, andthat is split to allow a reduction in size of the washer element.
 15. Asurgical fixation device, comprising: an annular portion having a bonecontact surface on a first side and an opening adapted to receive aligament repair material; and a securing portion attached to a secondside of the annular portion opposite the first side and having a portionthat extends across the opening of the annular portion, the securingportion having an elongated member extending in a direction away fromthe contact surface and being adapted to secure a ligament repairmaterial passing through the opening to the annular portion; wherein theannular portion and the securing portion are arranged to be deployedentirely within a bone opening and to resist tension applied on theligament repair material secured to the securing portion in a directionfrom the securing portion toward the contact surface.
 16. The device ofclaim 15, wherein a distal end of the elongated member located away fromthe annular portion has a groove to receive ligament repair material.17. The device of claim 15, wherein the elongated member of the securingportion includes opposed grooves to receive the joint repair material.18. The device of claim 15, wherein the securing portion includes one ormore openings adapted to receive suture to secure the ligament repairmaterial to the securing portion.
 19. The device of claim 15, comprisinga cylindrical portion that includes the annular portion and defines theopening, and wherein the elongated member has a wedge-like shape that isfixed to the cylindrical portion and extends across the opening.
 20. Thedevice of claim 15, wherein the securing portion extends across theopening and is attached to diametrically opposed portions of the annularportion.
 21. The device of claim 20, wherein the securing portion tapersso as to be thinner in a region near the opening and so as to be thickerin a region positioned away from the opening.
 22. The device of claim15, wherein the base and securing portions are made of an absorbablematerial.
 23. The device of claim 15, wherein the annular and securingportion are adapted to be used in a knee ligament repair procedure. 24.The device of claim 15, wherein the base and securing portion areadapted to be used in a knee ligament repair procedure using subcorticalbone fixation of the ligament.
 25. The device of claim 15, wherein theannular portion includes a washer element having a flange-like shape,that defines the contact surface, and that is split to allow a reductionin size of the washer element.